US1994702A - Utilization of waste pickling acids - Google Patents
Utilization of waste pickling acids Download PDFInfo
- Publication number
- US1994702A US1994702A US658156A US65815633A US1994702A US 1994702 A US1994702 A US 1994702A US 658156 A US658156 A US 658156A US 65815633 A US65815633 A US 65815633A US 1994702 A US1994702 A US 1994702A
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- US
- United States
- Prior art keywords
- tower
- towers
- acids
- ammonia
- utilization
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G49/00—Compounds of iron
- C01G49/02—Oxides; Hydroxides
- C01G49/06—Ferric oxide (Fe2O3)
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01C—AMMONIA; CYANOGEN; COMPOUNDS THEREOF
- C01C1/00—Ammonia; Compounds thereof
- C01C1/24—Sulfates of ammonium
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S423/00—Chemistry of inorganic compounds
- Y10S423/01—Waste acid containing iron
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S423/00—Chemistry of inorganic compounds
- Y10S423/01—Waste acid containing iron
- Y10S423/02—Sulfuric acid
Definitions
- This invention is a method or utilizing waste pickling acids. For instance, sulphuric or hydro- The new method is characterized'in: that the" waste pickling acids are treated with ammonia.
- the waste pickling acids are placed in towers, 1
- the ammonia replaces the iron atom and forms ferrous hydroxide which is oxidized by the oxygen in the air.
- the air also partially oxidizes the ferrous salts to the ferric state so that, as the addition of it and ammonia is continued, ferri-ferrous oxides are thrown out of solution.
- the tower 1 may be then refilled and the process rep ated after communication has been re- 20 established to the tower 2.
- the waste pickling acids in the tower 2 eventually react with the-gases unused in the tower 1, and are subjected to the separation already described. It is apparent that only one-tower may be used and the unused gases wasted or otherwise used, or that more towers than shown may be used to further insure the efiiciency of the process.
- This second-figure shows a constant level tower 13 to which the waste pickling acids are introduced by an inlet 14.
- An overflow pipe 15 maintains the liquid level.
- a pump 16 continuously delivers the acids from this tower through a feed valve 17 to the top of the first of a pair of reaction towers 18. The acids flow from the bottom of this tower and are delivered to the top of the second tower. This is preferably gravitationally efiected through a pipe 18 so that the levels in the two towers are at the same height.
- the valve 17 may be controlled by an automatic regulator 19 installed in either of the towers at the desired height.
- Both of the towers 18 are heated by steam coils 20 to temperatures in excess of 100 centigrade, and under counter pressures sufiiciently high to prevent boiling. These pressures may be maintained by compressed air which is introduced to the bottom of each tower by the pipe line 20 and held by a. pressure regulator 21. This regulator is inserted in a pipe 22 which interconnects the tops of the towers 18 and is arranged to introduce gases vented therefrom to the lower portion of the tower 13. Ammonia is also introduced to the first of the towers 18 by means of a pump 23.
- the treated pickling acids are withdrawn from the bottom of the second of the towers 18 and conveyed through a pipe 24 to a continuous filter 25 by way of a flash chamber 26.
- the level in the filter is preferably maintained by a float operated valve 27 positioned in the pipe 24.
- the filtrate is conveyed to a conventional evaporator 28 and from there to a crystallizer 29.
- the reactions are substantially the same as previously described. That is to say, the ammonia introduced to the acids in the first of the towers 18 replaces the iron atoms and forms ferrous hydroxide which is oxidized by the oxygen in the air which is simultaneously introduced.
- the heat from the coil 20 dehydrates the gelatinous precipitate to granular form.
- the ferrous salts in the acids are also partially oxidized by the air to the ferric state, so that as the addition of the air and ammonia is continued ferri-ferrous oxides are thrown out of solution.
- the completely precipitated and oxidized mixture leaves the bottom of the second of the towers and the granular iron oxides separated by the continuous filter 25.
- the filtrate contains ammonium salts which are separated by the evaporator 28 and solidified by the continuous crystallizer 29.
- the ammonium salts from; this crystallizer may be conveyed to a drain table or centrifugal dryer to condition them for handling.
- the method of treating waste pickling acids which includes the steps of continuously passing them successively through a plurality of towers, subjecting them to the action of ammonia, oxygen and heat while in one of said towers, subsequently subjecting them to the action of heat and oxygen while in another of said towers, re-
Description
March W, R935 A. w. HARRIS 3 UTILIZATION OF WASTE PICKLING ACIDS Filed Feb. 23, 1.933 2 Sheets-Sheet l MW /7/CH 14 HHEE/ March W, R935 A. W. HARRIS 2 UTILIZATION 6F WASTE PICKLING ACIDS Filed Feb. 23, 1933 2 Sheets-Sheet 2 QMWWMQnEG +1 MK EMF 3 n bl mRQwREMbEQD koi Patented Mar. 1 9, 1 93 I UNITE-D" STATES PATENT OFFICE 1,994,702 UTILIZATION or WASTE rroxnma Acms Arch W. diam-is, Par-ma; Ohio 1 Application February 23,-1933, S.erial,No. 658,156
1' Claim. (01. 235400) This invention is a method or utilizing waste pickling acids. For instance, sulphuric or hydro- The new method is characterized'in: that the" waste pickling acids are treated with ammonia.
and oxygen so that the ammonia replaces the iron and neutralizes the solution while the oxygen. causes the reaction to complete in an alkaline. solution and also oxidizes the ferrous ihydroxide to usable iron oxides. These reactionsare 'carm ried. out under sufficient heat to providerapid formation ofthe resulting precipitates and speedy oxidation and dehydration of the oxides, to assure the formation of the desired iron oxides in a granular form suitable for separation by filtration. Preferably, .the ammOniaisrecoVered insaltform. Y
the invention, and Figure 2 a modification whereby continuous operation is efiected. a
The waste pickling acids are placed in towers, 1
and 2 and heated by steam coils 3 to around 150 centigrade. Air at a pressure of from flto, 8 atmospheres is introduced. to the bottom of the tower by an air pump 4 through a suitably arranged line 5, along with ammonia from a constant pressure pump 6. The ammonia and air rising through the tower 1 are intimately mixedwith the hot waste pickling acids. The'counter pressure of the air existing in the tower 1 is sumcient to prevent boiling of the acids. V
The ammonia replaces the iron atom and forms ferrous hydroxide which is oxidized by the oxygen in the air. The air also partially oxidizes the ferrous salts to the ferric state so that, as the addition of it and ammonia is continued, ferri-ferrous oxides are thrown out of solution.
The process is continued until a sample of'the solution shows that the iron salts have been sub- 50 stantially if not entirely precipitated. This may be ascertained by testing with ammonium sulphide. vThe addition of ammonia is then discontinued and the air continued a suflicient time to drive out all excess ammonia.
The top of the tower 1 is interconnected to In the accompanying drawings,"Figure" L1vv grammatically illustrates one specific example of -paratus suitable for this purpose is illustrate by Figure 2.
the bottom of the-tower .2by a line 7 so that the gases from the first tower are introduced into the bottom of the second tower, and their loss prevented. This communication is maintainedwhile the above reactions-are being carried out 5 so that all unused ammonia is utilized by theacid in the tower 2. This second tower is provided with a relief valve 8 constructed to maintain the desiredcounter pressure in the two towers to prevent boiling of-the'liquids. 10
, When the precipitation in tower 1 is completed it is disconnected from tower 2'by a suitable valve and the resulting ammonium salt solution and iron oxides run through a pipe 9.to a filter 10. The filtrate is then sent to an evaporator 11 and 15 finally-to a centrifugal dryer 12 where the usable ammonium salts are dried. The desired iron oxides are, of course, obtained from the filter 10.
The tower 1 may be then refilled and the process rep ated after communication has been re- 20 established to the tower 2. The waste pickling acids in the tower 2 eventually react with the-gases unused in the tower 1, and are subjected to the separation already described. It is apparent that only one-tower may be used and the unused gases wasted or otherwise used, or that more towers than shown may be used to further insure the efiiciency of the process.
-O ne modification of the described method-may consist in effecting continuous operation. Ap-
This second-figure shows a constant level tower 13 to which the waste pickling acids are introduced by an inlet 14. An overflow pipe 15 maintains the liquid level. A pump 16 continuously delivers the acids from this tower through a feed valve 17 to the top of the first of a pair of reaction towers 18. The acids flow from the bottom of this tower and are delivered to the top of the second tower. This is preferably gravitationally efiected through a pipe 18 so that the levels in the two towers are at the same height. The valve 17 may be controlled by an automatic regulator 19 installed in either of the towers at the desired height.
Both of the towers 18 are heated by steam coils 20 to temperatures in excess of 100 centigrade, and under counter pressures sufiiciently high to prevent boiling. These pressures may be maintained by compressed air which is introduced to the bottom of each tower by the pipe line 20 and held by a. pressure regulator 21. This regulator is inserted in a pipe 22 which interconnects the tops of the towers 18 and is arranged to introduce gases vented therefrom to the lower portion of the tower 13. Ammonia is also introduced to the first of the towers 18 by means of a pump 23.
The treated pickling acids are withdrawn from the bottom of the second of the towers 18 and conveyed through a pipe 24 to a continuous filter 25 by way of a flash chamber 26. The level in the filter is preferably maintained by a float operated valve 27 positioned in the pipe 24. The filtrate is conveyed to a conventional evaporator 28 and from there to a crystallizer 29.
The reactions are substantially the same as previously described. That is to say, the ammonia introduced to the acids in the first of the towers 18 replaces the iron atoms and forms ferrous hydroxide which is oxidized by the oxygen in the air which is simultaneously introduced. The heat from the coil 20 dehydrates the gelatinous precipitate to granular form. The ferrous salts in the acids are also partially oxidized by the air to the ferric state, so that as the addition of the air and ammonia is continued ferri-ferrous oxides are thrown out of solution.
The air introduced to the second of the towers 18, this tower continuously receiving the liquids from the first, completes the oxidation and drives out the excess of ammonia. The vapors from the two towers are forced through the pipe 22 to the tower 13 where any unused ammonia or oxygen acts on the untreated acids.
The completely precipitated and oxidized mixture leaves the bottom of the second of the towers and the granular iron oxides separated by the continuous filter 25. The filtrate contains ammonium salts which are separated by the evaporator 28 and solidified by the continuous crystallizer 29. The ammonium salts from; this crystallizer may be conveyed to a drain table or centrifugal dryer to condition them for handling.
I claim:
The method of treating waste pickling acids, which includes the steps of continuously passing them successively through a plurality of towers, subjecting them to the action of ammonia, oxygen and heat while in one of said towers, subsequently subjecting them to the action of heat and oxygen while in another of said towers, re-
moving the vapors from said towers and subject-- ing the acids to the action of these vapors prior to their passage through these towers named, and finally subjecting them to filtration and evaporation.
ARCH W. HARRIS.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US658156A US1994702A (en) | 1933-02-23 | 1933-02-23 | Utilization of waste pickling acids |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US658156A US1994702A (en) | 1933-02-23 | 1933-02-23 | Utilization of waste pickling acids |
Publications (1)
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US1994702A true US1994702A (en) | 1935-03-19 |
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US658156A Expired - Lifetime US1994702A (en) | 1933-02-23 | 1933-02-23 | Utilization of waste pickling acids |
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Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2419240A (en) * | 1944-01-07 | 1947-04-22 | Nat Carbon Co Inc | Treating iron salt solutions |
US2443765A (en) * | 1945-07-02 | 1948-06-22 | Charles B Francis | Method for the utilization of spent pickling acid and crude coke works ammonia in the manufacture of ammonium sulfate and iron hydrates or oxides |
US2529874A (en) * | 1947-09-27 | 1950-11-14 | Mellon Inst Of Ind Res | Process for manufacturing ammonium salts and magnetic iron oxide from solutions of ferrous salts |
US2550425A (en) * | 1947-06-20 | 1951-04-24 | Standard Oil Dev Co | Suppression of corrosion |
US2605169A (en) * | 1948-05-26 | 1952-07-29 | Allied Chem & Dye Corp | Treatment of waste pickle liquor |
US2670271A (en) * | 1948-11-27 | 1954-02-23 | Alfred M Thomsen | Process of recovering metal values from leach liquors |
DE949571C (en) * | 1949-03-22 | 1956-09-20 | Chemische Werke Rombach G M B | Process for the production of ammonium sulphate, especially for fertilization purposes |
US2775508A (en) * | 1951-04-28 | 1956-12-25 | Alfred M Thomsen | Method of treating pickle liquors |
DE955773C (en) * | 1952-03-31 | 1957-01-10 | Chemische Werke Rombach G M B | Process for the production of ammonium sulphate, in particular for fertilization purposes |
US2939767A (en) * | 1957-10-07 | 1960-06-07 | Columbian Carbon | Manufacture of iron oxides |
US4935219A (en) * | 1986-12-17 | 1990-06-19 | Luis Escolar | Process for obtaining ferric oxide and ammonium salts |
US5013453A (en) * | 1983-03-21 | 1991-05-07 | Union Oil Company Of California | Method for removing heavy metals from aqueous solutions by coprecipitation |
US5045214A (en) * | 1983-03-21 | 1991-09-03 | Union Oil Company Of California | Methods for removing substances from aqueous solutions |
CN101177284B (en) * | 2007-11-02 | 2010-06-02 | 北京化工大学 | Method for reclaiming sulfuric ammonium and ferric oxide from sulfuric acid pickling waste fluid |
-
1933
- 1933-02-23 US US658156A patent/US1994702A/en not_active Expired - Lifetime
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2419240A (en) * | 1944-01-07 | 1947-04-22 | Nat Carbon Co Inc | Treating iron salt solutions |
US2443765A (en) * | 1945-07-02 | 1948-06-22 | Charles B Francis | Method for the utilization of spent pickling acid and crude coke works ammonia in the manufacture of ammonium sulfate and iron hydrates or oxides |
US2550425A (en) * | 1947-06-20 | 1951-04-24 | Standard Oil Dev Co | Suppression of corrosion |
US2529874A (en) * | 1947-09-27 | 1950-11-14 | Mellon Inst Of Ind Res | Process for manufacturing ammonium salts and magnetic iron oxide from solutions of ferrous salts |
US2605169A (en) * | 1948-05-26 | 1952-07-29 | Allied Chem & Dye Corp | Treatment of waste pickle liquor |
US2670271A (en) * | 1948-11-27 | 1954-02-23 | Alfred M Thomsen | Process of recovering metal values from leach liquors |
DE949571C (en) * | 1949-03-22 | 1956-09-20 | Chemische Werke Rombach G M B | Process for the production of ammonium sulphate, especially for fertilization purposes |
US2775508A (en) * | 1951-04-28 | 1956-12-25 | Alfred M Thomsen | Method of treating pickle liquors |
DE955773C (en) * | 1952-03-31 | 1957-01-10 | Chemische Werke Rombach G M B | Process for the production of ammonium sulphate, in particular for fertilization purposes |
US2939767A (en) * | 1957-10-07 | 1960-06-07 | Columbian Carbon | Manufacture of iron oxides |
US5013453A (en) * | 1983-03-21 | 1991-05-07 | Union Oil Company Of California | Method for removing heavy metals from aqueous solutions by coprecipitation |
US5045214A (en) * | 1983-03-21 | 1991-09-03 | Union Oil Company Of California | Methods for removing substances from aqueous solutions |
US4935219A (en) * | 1986-12-17 | 1990-06-19 | Luis Escolar | Process for obtaining ferric oxide and ammonium salts |
CN101177284B (en) * | 2007-11-02 | 2010-06-02 | 北京化工大学 | Method for reclaiming sulfuric ammonium and ferric oxide from sulfuric acid pickling waste fluid |
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